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Enzyme-free passage of human pluripotent stem cells by controlling divalent cations.


ABSTRACT: Enzymes used for passaging human pluripotent stem cells (hPSCs) digest cell surface proteins, resulting in cell damage. Moreover, cell dissociation using divalent cation-free solutions causes apoptosis. Here we report that Mg(2+) and Ca(2+) control cell-fibronectin and cell-cell binding of hPSCs, respectively, under feeder- and serum-free culture conditions without enzyme. The hPSCs were detached from fibronectin-, vitronectin- or laminin-coated dishes in low concentrations of Mg(2+) and remained as large colonies in high concentrations of Ca(2+). Using enzyme-free solutions containing Ca(2+) without Mg(2+), we successfully passaged hPSCs as large cell clumps that showed less damage than cells passaged using a divalent cation-free solution or dispase. Under the same conditions, the undifferentiated and early-differentiated cells could also be harvested as a cell sheet without being split off. Our enzyme-free passage of hPSCs under a serum- and feeder-free culture condition reduces cell damage and facilitates easier and safer cultures of hPSCs.

SUBMITTER: Ohnuma K 

PROVIDER: S-EPMC3983606 | biostudies-literature | 2014 Apr

REPOSITORIES: biostudies-literature

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Enzyme-free passage of human pluripotent stem cells by controlling divalent cations.

Ohnuma Kiyoshi K   Fujiki Ayaka A   Yanagihara Kana K   Tachikawa Saoko S   Hayashi Yohei Y   Ito Yuzuru Y   Onuma Yasuko Y   Chan Techuan T   Michiue Tatsuo T   Furue Miho K MK   Asashima Makoto M  

Scientific reports 20140411


Enzymes used for passaging human pluripotent stem cells (hPSCs) digest cell surface proteins, resulting in cell damage. Moreover, cell dissociation using divalent cation-free solutions causes apoptosis. Here we report that Mg(2+) and Ca(2+) control cell-fibronectin and cell-cell binding of hPSCs, respectively, under feeder- and serum-free culture conditions without enzyme. The hPSCs were detached from fibronectin-, vitronectin- or laminin-coated dishes in low concentrations of Mg(2+) and remaine  ...[more]

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